WIDE CORPORATION

FDA Device Registration & Listing · Hwaseong-si Gyeonggi, KR · Registration 3004082357

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3004082357
FEI Number
3004082357
Entity Name
WIDE CORPORATION
City/State/Country
Hwaseong-si Gyeonggi, KR
Establishment Address
15F, The First Tower III, 602 Dongtangiheung-ro, Hwaseong-si Gyeonggi 18469, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
WIDE CORPORATION (Owner Number: 9057040)
Owner / Operator Contact Address
15F, The First Tower III, 602 Dongtangiheung-ro, Hwaseong-si, KR-41 18469, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MX30N CX30N CX30N CX20N CX50N CW120N CW60N

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2016-05-13
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2021-04-14
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2016-05-13
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2016-05-13
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2017-04-10
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2021-04-08
PGY Display, Diagnostic Radiology Radiology Class 2 892.2050 2022-11-01

Official Correspondent

No official correspondent registered.

US Agent Details

isabell PARK Business: WIDE USA CORPORATION Email: ipark@foreseesonusa.com Phone: (714) 3000540

Related Public Records

Same Entity

WIDE CORPORATION
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K163335 Eizo Corporation 6MP Color LCD Monitor, RadiForce RX660, RX660-AR 2016-12-15

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3004082357. Last updated year: 2026. Please use registration number 3004082357 when referencing this establishment in official correspondence.
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